dichlorfop-methyl has been researched along with haloxyfop in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Casida, JE; Kemal, C | 1 |
| Beaudoin, JD; Craig-Kennard, AC; Felts, JM; Hagenah, JA; Look, LL; Paraskos, SL; Rendina, AR | 1 |
| Neve, P; Powles, S | 1 |
| Dong, W; Fang, Y; Jiang, M; Liu, K; Ma, J; Xin, F; Xu, N; Zhang, W; Zhou, J | 1 |
1 review(s) available for dichlorfop-methyl and haloxyfop
| Article | Year |
|---|---|
Recent insights into the microbial catabolism of aryloxyphenoxy-propionate herbicides: microbial resources, metabolic pathways and catabolic enzymes.
Topics: Anilides; Bacteria; Benzoxazoles; Biodegradation, Environmental; Butanes; Dihydropyridines; Halogenated Diphenyl Ethers; Herbicides; Metabolic Networks and Pathways; Microbial Consortia; Nitriles; Oxazoles; Propionates; Pyridines; Quinoxalines; Soil Microbiology | 2018 |
3 other study(ies) available for dichlorfop-methyl and haloxyfop
| Article | Year |
|---|---|
Coenzyme A esters of 2-aryloxyphenoxypropionate herbicides and 2-arylpropionate antiinflammatory drugs are potent and stereoselective inhibitors of rat liver acetyl-CoA carboxylase.
Topics: Acetyl-CoA Carboxylase; Animals; Binding Sites; Coenzyme A; Dihydropyridines; Esters; Fenoprofen; Halogenated Diphenyl Ethers; Herbicides; Ibuprofen; Kinetics; Liver; Male; Phenyl Ethers; Pyridines; Rats; Rats, Inbred Strains; Stereoisomerism; Structure-Activity Relationship | 1992 |
Kinetic characterization, stereoselectivity, and species selectivity of the inhibition of plant acetyl-CoA carboxylase by the aryloxyphenoxypropionic acid grass herbicides.
Topics: Acetyl-CoA Carboxylase; Drug Tolerance; Halogenated Diphenyl Ethers; Herbicides; Kinetics; Ligases; Phenyl Ethers; Plants; Plants, Toxic; Pyridines; Ricinus communis; Species Specificity; Stereoisomerism; Structure-Activity Relationship; Triticum | 1988 |
Recurrent selection with reduced herbicide rates results in the rapid evolution of herbicide resistance in Lolium rigidum.
Topics: Crosses, Genetic; Cyclohexanones; Dose-Response Relationship, Drug; Drug Resistance; Evolution, Molecular; Halogenated Diphenyl Ethers; Herbicides; Lethal Dose 50; Lolium; Nicotinic Acids; Phenotype; Phenyl Ethers; Pyridines; Selection, Genetic | 2005 |